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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599298Generated: October 31, 2026

Hydrochloric Acid → HCID 86629455, compound

https://huagongshe.com/reaction/599298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 86629454HCID 86629454—
CatalystIronHCID 23925—
SolventWater ethanolHCID 19096565—
ProductHCID 86629455HCID 8662945562%

Reaction Conditions

Temperature40 °C

Reaction Steps

Iron powder was added (5.2 g, 93 mmol) in portions to a solution of 1-tert-butyl-7-chloro-3-(4-fluoro-3-nitrophenyl)-3,4-dihydropyrido[4,3-d]pyrimidin-2(1H)-one (3.5 g, 9.3 mmol) and conc. HCl (0.35 mL, 4.2 mmol) in 10/1 EtOH/H2O (11 mL). The resulting mixture was stirred at 40° C. for 30 min. The reaction mixture was filtered and the filter cake was washed with EtOH. The ethanolic filtrate was concentrated and the residue was partitioned between EtOAc and H2O. The aqueous layer was extracted with EtOAc (3×80 mL). The combined organics were washed with brine, dried (Na2SO4), concentrated in vacuo and purified by chromatography on silica gel to afford 3-(3-amino-4-fluorophenyl)-1-tert-butyl-7-chloro-3,4-dihydropyrido[4,3-d]pyrimidin-2(1H)-one (2.0 g, 62% yield). 1HNMR (400 MHz, DMSO-d6): δ 8.20 (s, 1 H), 7.26 (s, 1 H), 6.92 (m, 1 H), 6.62 (m, 1 H), 6.34 (m, 1 H), 5.17 (s, 2 H), 4.50 (s, 2H), 1.55 (s, 9 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897762B2
Source datasetuspto-grants-2011_03
ORD IDord-8e80c59f22424538aa947730d8dbbaa4
Source noteuspto-grants-2011_03